ライフサイエンスコーパス: 3D

1 3D Caco-2 models treated with EGF had increased glucose

2 3D hepatic microtissues, unlike 2D cell cultures, retain

3 3D imaging of the bone vasculature is of key importance

4 3D matrix made by laser engraving of polymethyl methacry

5 3D porous nanostructures built from 2D delta-MnO2 nanosh

6 3D printing has been developed for a variety of applicat

7 3D protein modeling revealed that the 3 variants affect

8 remolars retained 67-68%, 39-41%, and 15-17% 3D BA-RSA, respectively.

9 The coronal 30%-31% 2D RL and the 41%-42% 3D RSA bone loss corresponded to a CRR of 5:4, correlati

10 A 3D array of organic semiconductors was assembled using a

11 A 3D continuum model of the embryo with induced contractil

12 A 3D potential energy surface generated for this reaction

13 A 3D printed cradle held the smartphone integrated with op

14 In this study, we 1) defined a 3D stereotaxic coordinate system for previously establis

15 Here, we describe a 3D printed inexpensive open source and scalable motorize

16 aps because of the challenge of estimating a 3D function from perceptual reports in psychophysical ta

17 images to the third dimension, we examined a 3D image stack from serial-section TEM (ssTEM) of the op

18 The protocol for generating a 3D construct takes 6 weeks to complete, and it requires

19 -culture of tumor and endothelial cells in a 3D environment.

20 ach image, accurately assembling them into a 3D diffraction intensity function, and determining missi

21 TAD boundary mediate de novo formation of a 3D contact domain comprising IGF2 and a lineage-specific

22 ique in vitro method for the generation of a 3D human lymphatic network within native connective tiss

23 ror-symmetry breaking and the emergence of a 3D inverse cascade.

24 m embedding the strings in the interior of a 3D manifold with boundary.

25 Our tool further created browsable maps of a 3D microbiome/metabolome reconstruction map on a radiolo

26 We report the development of a 3D OrbiSIMS instrument for label-free biomedical imaging

27 Here, we report the design of a 3D topological metamaterial without Weyl lines and with

28 Two versions of a 3D-printed cartridge for paper spray ionization (PSI) ar

29 Our design is based on a 3D-printed mainframe, a Raspberry Pi computer, and high-

30 ging network is energetically favored over a 3D network, driving the formation of NPLs.

31 nect two nonsister chromatids, and present a 3D model of the Drosophila SC based on these findings.

32 Here, we report a 3D microfluidic platform that could be potentially used

33 FB:EC = 70:15:15, 70:0:30, 45:40:15) using a 3D bioprinter.

34 Using a 3D particle tracking method, the authors show that the s

35 cy at comparable residence time and, using a 3D-printed interface, be directly interfaceable with LC-

36 atural product macrocycle upon its activity, 3D geometry, and conformational entropy.

37 Here, by using advanced 3D fabrication techniques we integrated a microbead on a

38 ux, Inc., Durham, NC) compared to BacT/Alert 3D (BTA3D) for detection of bacteremia/fungemia in four

39 contact-guided migration of CSCs in aligned 3D collagen matrices.

40 pologically distinct band-structures for all 3D space groups.

41 Also, 3D-printed muSPE devices enabled fast emulsion breaking

42 eas, but the construction of objects, 2D and 3D crystalline lattices and devices is prominent among t

43 lasma membrane and filopodia, and the 2D and 3D dynamics of the endoplasmic reticulum, in living cell

44 Weyl fermions can be realized in both 2D and 3D materials.

45 sive characterizations, extensions to 2D and 3D trajectories, and applications to common scenarios ar

46 thirteen consecutive renal transplant 2D and 3D ultrasound examinations were performed and retrospect

47 Here we use 2D and 3D X-ray imagery on Noril'sk nickel sulfide, combined wi

48 Serial ultrathin section analysis and 3D reconstructions revealed that Ank-G colocalized with

49 id chromatographic columns were designed and 3D printed in titanium as 2D serpentine, 3D spiral, and

50 patients underwent TRUS, T1W, T2W, DWI, and 3D PRESSMRS sequences, and we also calculated ADC values

51 study, by combining immunohistochemistry and 3D ultrastructural analyses, we show that mitochondrial

52 survival were not different between IMRT and 3D-CRT.

53 tion microscopy to measure the magnitude and 3D orientation of cellular forces.

54 ultivariate statistical analysis methods and 3D reconstruction approaches originally developed for cr

55 of human melanopsin, confocal microscopy and 3D reconstruction of melanopsin immunoreactive (-ir) RGC

56 activation, mitotic spindle orientation and 3D glandular morphogenesis.

57 To demonstrate this concept, planar and 3D-structured sheets are preprogrammed to evolve into bi

58 mechanisms that connect gene regulation and 3D epithelial morphogenesis.

59 periodontitis on the basis of the 2D RL and 3D RSA measurements.

60 of an atlas including confocal sections and 3D digital models for the larval, pupal and adult stage,

61 analyses of DNase I-hypersensitive sites and 3D genome architecture, linking functional variants to g

62 in titanium as 2D serpentine, 3D spiral, and 3D serpentine columns, of equal length and i.d.

63 nd fibres, 2D films and coated surfaces, and 3D patterned surfaces such as pillars.

64 selective arterial spin labeling (VSASL) and 3D image acquisition with whole-placenta coverage.

65 As 3D fluorescence techniques are commonly applied to diver

66 l of DNA nanotechnology has been to assemble 3D crystals to be used as molecular scaffolds.

67 s are fabricated by an electrically assisted 3D-printing method.

68 idermal keratins 1 and 10, based on all-atom 3D simulations of keratin primary amino acid sequences,

69 move on a spherical nucleic acid (SNA)-based 3D track.

70 They could be 3D printed and cured both in air and under water.

71 strategy to illuminate the interplay between 3D chromatin structure and epigenetic dynamics.

72 opments in microscale devices and bioprinted 3D tissues are beginning to supplant traditional 2D cell

73 ion into polyrotaxane-based lattice cubes by 3D printing followed by post-printing polymerization are

74 devices are further demonstrated, enabled by 3D printing of programed cells, including logic gates, s

75 Z domain-ligand interaction was explained by 3D structural models, which showed a hormone-regulated m

76 tainless steel electrodes were fabricated by 3D printing, and the surface was electroplated with gold

77 erograde tracer, AAV-SynaptoTag, followed by 3D reconstruction of the cortical projections, we perfor

78 al for exposure to the aerosols generated by 3D printers under real-use conditions in a variety of in

79 ying dielectric permittivity manufactured by 3D printing.

80 il aggregate fractal properties supported by 3D microtomographic imagery, we found that N fertilizati

81 The data are underpinned by 3D numerical simulations which suggest that in these con

82 nzyme conformational change was validated by 3D fluorescence and CD spectrum.

83 Here we calculate 3D structures of entire mammalian genomes using data fro

84 The method is called 3D-SDAR (3-dimensional spectral data-activity relationsh

85 Comparative 3D analysis with dense sampling offers a precise methodo

86 orrelation analysis are then used to compare 3D expression patterns, to automatically detect all stat

87 This study compares 3D-CRT and IMRT outcomes for locally advanced NSCLC in a

88 ct 3D printing of layer-by-layer and complex 3D microscale nt-Cu structures, which may find applicati

89 monstrate laser-based fabrication of complex 3D structures deep inside silicon using 1 microm-sized d

90 ovides a challenge for probing their complex 3D conformational landscape, both experimentally and com

91 T growth speeds in ECs cultured on compliant 3D ECMs, and these effects are myosin-II dependent.

92 rrent study, a novel platform for conducting 3D cell culture and analyzing cell viability has been de

93 the present study, we aimed at constructing 3D neurovascular tissues by combining in vitro neurogene

94 Conventional 3D bioprinting allows fabrication of 3D scaffolds for bi

95 range of applications for the cryogenically 3D printed CH structures, from soft tissue phantoms for

96 The custom 3D printing of functional materials and devices opens ne

97 a paradigm for creating actively deployable 3D structures with complex shapes.

98 wo distinct approaches for stem cell-derived 3D tissue preparation.

99 Detailed 3D analysis of their structural organization allowed a f

100 Here, we developed 3D cell-line-based models of human syncytiotrophoblasts,

101 microfluidic paper-based analytical devices (3D-muPADs) are an evolution of single layer devices and

102 RATIONALE: Conventional 3-dimensional (3D) printing techniques cannot produce structures of the

103 rsed surface accumulation three dimensional (3D) printing process.

104 We report a three dimensional (3D) quantitative visualization of a mammalian mitochondr

105 Three - dimensional (3D) electrodes are successfully used to overcome the lim

106 The three-dimensional (3D) architecture of the cell nucleus plays an important

107 ns in human body, such as three-dimensional (3D) architecture, cell heterogeneity, nutrient gradients

108 Three-dimensional (3D) assemblies based on carbon nanomaterials still lag b

109 on, their applications to three-dimensional (3D) biomolecular structural data sets have been hindered

110 shared interest in using three-dimensional (3D) culture methods to study biology, model disease and

111 plies the importance of a three-dimensional (3D) culture model including these cell types for investi

112 227E)-expressing cells in three-dimensional (3D) culture.

113 submillimetric layers of three-dimensional (3D) cultures.

114 Here, using three-dimensional (3D) electron diffraction mapping approach, we non-destru

115 r growth in a controlled, three-dimensional (3D) environment.

116 formed to realise various three-dimensional (3D) geometries.

117 cell (NPC) culture within three-dimensional (3D) hydrogels is an attractive strategy for expanding a

118 viour of the film and the three-dimensional (3D) magnetic structure of nano-rods.

119 ogrammable fabrication of three-dimensional (3D) materials by printing engineered self-patterning bac

120 Three-dimensional (3D) models of dimers are generated by threading a target

121 Three-dimensional (3D) molecular imaging enables the study of biological pr

122 Three-dimensional (3D) optical imaging of whole biological organs with micr

123 Three-dimensional (3D) ordered arrays of human immunoglobulin G (IgG) were

124 A unique three-dimensional (3D) organotypic culture model was established; within a

125 Three-dimensional (3D) printing has proven to be a versatile and useful tec

126 techniques, for example, three-dimensional (3D) printing, of all-liquid constructs.

127 devices via multimaterial three-dimensional (3D) printing.

128 relationship between the three-dimensional (3D) root surface area (RSA) and two-dimensional (2D) cro

129 t upon sustained specific three-dimensional (3D) structures of RNA, with or without the help of prote

130 We describe herein a three-dimensional (3D) tissue culture platform using a polydimethylsiloxane

131 Bioengineered three-dimensional (3D) tumor models that incorporate heterotypic cellular c

132 Three-dimensional (3D) tumor spheroid models have gained increased recognit

133 The L-PED process enables direct 3D printing of layer-by-layer and complex 3D microscale

134 acking process, then allows highly efficient 3D OCT and fluorescence imaging by using only one raster

135 low carbon utilization, a highly efficient, 3D solid-state architected anode is developed to enhance

136 rates, the new process reported here enables 3D control over the shape and thickness of the removed r

137 l-based approach to generate endothelialized 3D vascular networks within cell-laden hydrogel biomater

138 Thus, the novel multiphoton-excited 3D printing technique produces extracellular matrix-base

139 D printing approach is employed to fabricate 3D tactile sensors under ambient conditions conformally

140 D (DPMD) method that measures the full-field 3D shape of complicated specular objects.

141 ting method, and the structures of the final 3D-printed products.

142 le inks are the most important component for 3D printing, and are related to the materials, the print

143 new open source cluster analysis method for 3D SMLM data, free of user definable parameters, relying

144 In appropriate conditions, CSC form 3D spheres (SPH), which retain stem-like tumour-initiati

145 d ferritin proteins for printing and forming 3D shapes and structures.

146 Fragile 3D floc samples were successfully captured and stabilize

147 low-coherence interferometry for label-free 3D imaging in scattering tissue.

148 otoacoustic microscopy allows for label-free 3D in vivo imaging by detecting the acoustic response of

149 These methods allow for the reference-free 3D reconstruction of nanomolecular structures from two-d

150 From 3D visualization, gap progress could be seen on both ena

151 ing, drinking, and locomotor activities from 3D trajectories.

152 mography method is employed to obtain a full 3D structural dataset of the network morphology within a

153 s is the first demonstration of a functional 3D CMOL hybrid circuit.

154 beating cardiomyocytes provides a functional 3D map of active ECC couplons (on average, 17,000 per my

155 hesin and condensin establish the functional 3D genome structures.

156 Furthermore, the hybrid 3D additive printing strategy for biosensors facilitates

157 ination of approaches (non-invasive imaging, 3D-electron microscopy, and mathematical modelling) to s

158 In 3D collagen matrix, RhoA knockout reduced fibroblast bra

159 roliferation of MM cells in monolayer and in 3D sponges but did not affect MM cell migration, organiz

160 It is also now integrated with built-in 3D visualization which interacts with the formatted alig

161 c anti-PD-1 antibody increased cell death in 3D spheroids and extended survival of MDA-MB-231-bearing

162 so show that iRFP can be readily detected in 3D organoid cultures, FACS analysis and in vivo tumour m

163 Lithium niobate crystals were grown in 3D through localized heating by femtosecond laser irradi

164 he invasion of prostate cancer cell lines in 3D in vitro assays.

165 lizable strategy for stemness maintenance in 3D.

166 Studies of carbon materials in 3D printing, especially GO-based materials, have been ex

167 erm in vivo monitoring the mineralization in 3D scaffolds subcutaneously implanted in small animals.

168 ic method to identify these modifications in 3D protein structures.

169 ng randomly distributed groups of neurons in 3D.

170 0 nm in 2D electron microscopy and 3.3 nm in 3D electron tomography indicates a genuine signalling mi

171 re kinetics of different nanoscale phases in 3D, and reveals insights behind some of the observed nov

172 e presence of intrinsic 2D Dirac plasmons in 3D nanoporous graphene disclosing strong plasmonic absor

173 Progress in 3D electron microscopy (EM) imaging has greatly facilita

174 unified account of long-standing puzzles in 3D vision at the physiological and perceptual levels.

175 diverse sorghum lines were reconstructed in 3D for feature extraction.

176 upported long-term epidermal regeneration in 3D organotypic cultures, and resulted in the manifestati

177 somal interactions play an important role in 3D chromosome structure and function, but our understand

178 agents that share significant similarity in 3D shape and surface electrostatics with few, hitherto b

179 lipid bodies and cytoskeletal structures in 3D with unprecedented biomolecular specificity for vibra

180 d endogenous metabolites to be visualized in 3D with subcellular resolution.

181 An innovative 3D growth platform, which enabled the FTE organoid to se

182 new class of nanoobjects with an intriguing 3D architecture.

183 cations of the methodology for investigating 3D spheroid morphology and marker expression and for in

184 a function of crystal orientation in a laser 3D-printed DL125L Ni-based superalloy polycrystal is inv

185 -metallic structure was fabricated via laser 3D printing following the transition route.

186 evice, including a comprehensive parts list, 3D design files in STEP (Standard for the Exchange of Pr

187 ch as hyper-spectral imaging, depth mapping, 3D profiling.

188 lation microscopy, to quantitatively measure 3D protein dynamics in the nucleus.

189 A hot melt 3D inkjet printing method with the potential to manufact

190 ltimaterial, multiscale, and multifunctional 3D printing approach is employed to fabricate 3D tactile

191 New 3D spherical numerical models embedded with the latest g

192 A novel 3D Co-Nx |P-complex-doped carbon grown on flexible exfol

193 In contrast, the sensitivity to object 3D structure remains stable even through late adulthood

194 ltaneously provided comprehensive details of 3D morphological changes of the IVD and canal network in

195 Here we report the development of 3D imaging cluster Time-of-Flight secondary ion mass spe

196 ntional 3D bioprinting allows fabrication of 3D scaffolds for biomedical applications.

197 Structural features of 3D-reconstructed eukaryotic cells that are affected by D

198 With the growth of 3D packaging technology and the development of flexible,

199 In an in vitro model of 3D microvessels, both tumor-derived and matched normal L

200 r more efficient and versatile production of 3D objects.

201 hydrodynamics requires the quantification of 3D floc properties (size, shape, density and porosity) t

202 on, for the first practicable realisation of 3D photonic microstructure shaping based on 2D-fluid com

203 olithography demonstrates the scalability of 3D structures.

204 on diverse fields ranging from the study of 3D atomic arrangements in matter to the study of human h

205 Herein, we report the novel synthesis of 3D graphitic carbon networks through the pyrolysis of na

206 optimal countershading transitions based on 3D reconstructions of the animal's abdomen, imaged in di

207 cient bifunctional electrocatalysts based on 3D transition-metal-based materials for oxygen evolution

208 es the reproducibility of tests performed on 3D-muPADs.

209 iple, degenerate, interchangeable, linear or 3D hydrophobic stretches that become available because o

210 portunities for the rational design of other 3D transition-metal-based electrocatalyst through an out

211 dynamically assemble into a fully percolated 3D network within high-concentration protein polymers.

212 These unique high-performance 3D structures offer potential in fields ranging from wat

213 Peripapillary 3D RNFL volume parameters have the same or better diagno

214 Peripapillary 3D RNFL volume showed excellent diagnostic performance f

215 Peripapillary 3D RNFL volumes were calculated for global, quadrant, an

216 us, for the first time, to map the physical 3D structure of previously inaccessible habitats and dem

217 rategy for the fabrication of an open porous 3D self-organized double-hierarchical carbon nanotube tu

218 metal processing on a single high-precision 3D stage.

219 This does not prevent 3D systems from being glassy.

220 present the rational design of a wax-printed 3D-muPAD that enables more homogeneous permeation of flu

221 the required fabrication times for producing 3D, hierarchical microstructures over large areas in the

222 his work opens new directions in programming 3D shapes by providing new insight into helical segments

223 This system can potentially provide 3D bio-interfaces such as those needed for reconstructio

224 ed analysis pipeline to analyze and quantify 3D-SIM images and generate a population-level descriptio

225 ovel array of quasi-three-dimensional (quasi-3D) bowtie nanoantennas has been investigated numericall

226 ting lattice component can evolve from quasi-3D to quasi-1D, leading to strong Fermi surface mismatch

227 tours of the metamaterials made of the quasi-3D bowtie nanoantennas, respectively.

228 formability attributed to the reconfigurable 3D network from stiff collagen nanofibers and flexible p

229 g macrosection images yields high resolution 3D maps of multiple tumor microenvironment components an

230 We built a quality high-resolution 3D atlas of average in vivo sheep brains linked to a ref

231 copy (SIM), we have captured high-resolution 3D images showing MOF uptake by HeLa cells over a 24 h p

232 Econstruction (GENFIRE), for high-resolution 3D reconstruction from a limited number of 2D projection

233 corporates this information into current RNA 3D structure prediction methods, specifically 3dRNA.

234 poral patterns, we constructed a large-scale 3D network model of the granular layer.

235 and 3D printed in titanium as 2D serpentine, 3D spiral, and 3D serpentine columns, of equal length an

236 nd phosphate, also act as signals that shape 3D root growth to optimise uptake.

237 n primary sequence, but cluster into a small 3D putative binding site.

238 ion both on epitope data derived from solved 3D structures, and on a large collection of linear epito

239 A three-dimensional structure (3D) model of Ss-RIOK-2 was generated using the Chaetomiu

240 fy and to fix likely errors in user supplied 3D models of proteins via successive rounds of refinemen

241 Our study demonstrates that 3D electron diffraction mapping is a powerful tool for t

242 Furthermore, we find that 3D ECM engagement uncouples MCAK-mediated regulation of

243 t this work is an example of the impact that 3D-printing will have on the future of analytical device

244 Here the authors show that 3D collagen gels, major components of connective tissues

245 Here we show that 3D collagen gels, major components of connective tissues

246 The 3D microfluidic chip reduces reactant consumption and fa

247 The 3D model was positioned above the surgical site.

248 The 3D printed nt-Cu is fully dense, with low to none impuri

249 The 3D scanning was performed 0, 1, 3, 5, and 10 min after l

250 The 3D shape of the droplets was imaged as a function of the

251 Here we determine the 3D coordinates of 6,569 iron and 16,627 platinum atoms i

252 f materials it is necessary to determine the 3D positions of all atoms.

253 Finally, the 3D trajectories and the accompanying rotational motions

254 ally driven smooth eye movements to find the 3D space-time function that best predicts both eye movem

255 al attachment loss (CAL) was observed in the 3D RSA measurement than in the 2D RL measurement at the

256 eta-6 complexes revealed similarities in the 3D structures of bound partner proteins, suggesting the

257 chieved in virtue of the Ag nanoseeds in the 3D substrate, showing a low overpotential ( approximatel

258 rstanding of how the genome folds inside the 3D nucleus and how these folding patterns are miswired d

259 er-resolution microscopy, we have mapped the 3D spatial locations of transport routes for various cyt

260 en passes through the minimum that marks the 3D-2D crossover in the system.

261 dered by the need for spatial imaging of the 3D fields, which is difficult in high-energy physics and

262 h demonstrated not only the potential of the 3D printing environment in planar chromatography but als

263 provide guidance toward the selection of the 3D printing technology most suitable for specific microf

264 both growth and melting morphologies of the 3D quasicrystal at temperature.

265 Use of the 3D serpentine column at a higher flow rate, as compared

266 The high stability of the 3D Star of David was correlated to its high density of c

267 ethod must be implemented to reconstruct the 3D structure of an object from a number of 2D projection

268 n of the nuclear piston mechanism slowed the 3D movement of HT1080 cells.

269 od was further validated by showing that the 3D printed material was well matched to the cast-moulded

270 mn at a higher flow rate, as compared to the 3D spiral column, provided a 58% reduction in the analys

271 Starting with the 3D genome organization map of LCL, we constructed a comp

272 The cell with the 3D textile anode framework, Gd:CeO2 -Li/Na2 CO3 composit

273 However, protein dynamics within the 3D nucleus are poorly understood.

274 dent individually; each reviewed 2D and then 3D images, including color and spectral Doppler.

275 l conformal external beam radiation therapy (3D-CRT) have not been compared prospectively.

276 used as anodes for sodium-ion storage, these 3D MXene films exhibit much improved performances compar

277 direct experimental comparison of the three 3D printing technologies dominating microfluidics was co

278 rformance based on available sensory cues to 3D motion.

279 Recently, SMLM has been extended to 3D, providing a unique insight into cellular machinery.

280 and then analyzed for cellular responses to 3D hypoxic gradients and to elucidate the underlying mec

281 Here, we translate 3D-microscopy techniques (focused ion beam nanotomograph

282 h Ficus species is characterized by a unique 3D mineral distribution that is preserved in different e

283 isordered proteins (IDPs) that lack a unique 3D structure and comprise a large fraction of the human

284 Here, we use 3D direct stochastic optical reconstruction microscopy (

285 e association study for molar shape and used 3D surface morphometrics to quantify subtle variation be

286 Using 3D full-waveform tomography, we reveal an expansive low-

287 d a novel method to deliver stem cells using 3D bioprinted cardiac patches, free of biomaterials.

288 n 29 species of living and fossil deer using 3D geometric morphometrics and cladistics.

289 y the resulting directional resolution using 3D Fourier shell correlation volumes.

290 nergy cascade in an experimentally validated 3D active fluid model, describing microbial suspension f

291 ht modulate the release of paused RNAPII via 3D chromatin looping.

292 pulations in intact Ce3D-treated tissues via 3D histo-cytometry.

293 By using a high-speed virtual 3D super-resolution microscopy, we have mapped the 3D sp

294 ces arise at a level of representation where 3D shape is made explicit.

295 CaCLEAN combined with 3D confocal imaging of beating cardiomyocytes provides a

296 Coarse-grained models are compared with 3D cryo-electron microscopy density maps for these five

297 ivo functional ovarian implant designed with 3D printing, and indicate that scaffold pore architectur

298 mework that couples 1D genomic features with 3D interactions from Hi-C to probe the guiding principle

299 of the entire anastomosis was improved with 3D ultrasound.

300 when coupled to membrane composition yields 3D bicontinuous cubic phases that swell up to lattice di